首页> 外文期刊>Virology: Research and Treatment >Antibiotic-Mediated Inhibition of Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Infection: A Novel Quinolone Function Which Potentiates the Antiviral Cytokine Response in MARC-145 Cells and Pig Macrophages
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Antibiotic-Mediated Inhibition of Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Infection: A Novel Quinolone Function Which Potentiates the Antiviral Cytokine Response in MARC-145 Cells and Pig Macrophages

机译:抗生素介导的猪繁殖与呼吸综合征病毒(PRRSV)感染的抑制:一种新型喹诺酮功能,可增强MARC-145细胞和猪巨噬细胞的抗病毒细胞因子反应。

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Porcine reproductive and respiratory syndrome virus (PRRSV) is an economically significant agent for which there currently are no effective treatments. Development of antiviral agents for PRRSV as well as many other viruses has been limited by toxicity of known antiviral compounds. In contrast, antibiotics for non-virus microbial infections have been widely useful, in part because of their acceptable toxicity in animals. We report here the discovery that the quinolone-containing compound Plasmocin ?¢???¢ , as well as the quinolones nalidixic acid and ciprofloxacin, have potent anti-PRRSV activity in vitro. PRRSV replication was inhibited by these antibiotics in both cultured MARC-145 cells and cultured primary alveolar porcine macrophages (PAMs). Furthermore, sub-optimal concentrations of nalidixic acid synergized with antiviral cytokines (AK-2 or IFN-???3) to quantitatively and qualitatively inhibit PRRSV replication in MARC-145 cells or PAMs. The antiviral activity of Plasmocin and nalidixic acid correlated with reduced actin expression in MARC-145 cells. Replication of the related lactate dehydrogenase-elevating virus (LDV) was also inhibited in primary mouse macrophages by Plasmocin. These results are significant to the development of antiviral strategies with potentially reduced toxicity, and provide a model system to better understand regulation of arterivirus replication.
机译:猪繁殖与呼吸综合症病毒(PRRSV)是一种经济上重要的药物,目前尚无有效的治疗方法。用于PRRSV以及许多其他病毒的抗病毒剂的开发受到已知抗病毒化合物毒性的限制。相反,用于非病毒微生物感染的抗生素已被广泛使用,部分原因是它们对动物具有可接受的毒性。我们在这里报告发现含喹诺酮的化合物Plasmocin?,以及喹诺酮类萘啶酸和环丙沙星在体外具有有效的抗PRRSV活性。这些抗生素在培养的MARC-145细胞和培养的初级肺泡猪巨噬细胞(PAM)中均抑制PRRSV复制。此外,亚最佳浓度的萘啶酸与抗病毒细胞因子(AK-2或IFN-γ3)协同作用,以定量和定性抑制MARC-145细胞或PAM中的PRRSV复制。 Plasmocin和萘啶酸的抗病毒活性与MARC-145细胞中肌动蛋白表达降低有关。 Plasmocin在原代小鼠巨噬细胞中也抑制了相关的乳酸脱氢酶升高病毒(LDV)的复制。这些结果对于开发具有潜在降低的毒性的抗病毒策略具有重要意义,并提供了一个模型系统以更好地理解动脉病毒复制的调控。

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